Michelle Tarver
Tracked across 2 events · 14 articles · First seen Jun 13, 2026 · Last active Aug 20, 2026
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Regulatory
Impact: Michelle Tarver, director of the United States — Food and Drug Administration's Center for Devices and Radiological Health, commented on the importance of the clearance for pediatric patients.
Jun 13, 2026 · 7 articles
Regulatory
The U.S. United States — Food and Drug Administration (FDA) has granted marketing authorization to Vitestro for the Aletta, the first standalone robotic device capable of drawing blood from a patient's arm without hands-on operator…
Impact: Michelle Tarver, Director of the FDA's Center for Devices and Radiological Health, publicly endorsed the authorization, highlighting its role in addressing the phlebotomist shortage. Her statement underscores the FDA's support for the device, though her personal impact is limited to her official role.
Aug 19, 2026 · 7 articles
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